Sentence examples for controls eligibility from inspiring English sources

Forms included selection forms for visitor controls, eligibility forms for IBC and non-IBC cases, consent forms, the questionnaire, clinical examination forms, medical record review forms, pathology report forms, instructions for saliva collection and anthropometric measurements, and taking digital photographs.

Also, each node has a critic agent which evaluates the control eligibility of the low-level controllers for controlling the system.

Details of CBC case and UBC control eligibility have been described previously [ 16].

Control eligibility criteria included a) not having PD, b) ≥ 35 years of age, and c) currently residing in one of the three counties and having lived in California for at least 5 years before our screening.

Interviewing women who had recently been pregnant and their husbands controls for eligibility for those services.

For the normal controls (NC's) eligibility was if they had no history of ever having suffered a chronic illness and were ≥ 18 years of age.

Patients selected for self-management within these studies were inherently more likely to have better therapeutic control as eligibility would include levels of 'intelligence', manual dexterity and previously stable control.

However, when controlling for eligibility and pre-birth employment characteristics the gradient disappears.

Mr. Obama would expand Medicaid to cover millions more people; Mr. Romney would effectively shrink it, giving each state a fixed amount of federal money to cover its disadvantaged population with more control over eligibility and benefits.

Mr. Romney and Republicans in Congress want to repeal the health care law and replace the current Medicaid program with block grants, giving each state a fixed amount of federal money each year and more control over eligibility and benefits.

This paper presents a tutorial on RCTs, presenting and discussing the following principles and methods: the trial protocol, choice of control treatment, eligibility criteria, random allocation, outcomes and hypotheses, sample size, subject recruitment, analysis by intention to treat, interim analysis, stopping rules, safety data monitoring/trial management, and study documentation.